Alprazolam
- Product NDC
- 50090-5261
- 11-digit product format
- 500905261
- Labeler code
- 50090
- Product ID
- 50090-5261_6ab4f438-9ff6-4749-ab95-1c6bf481d542
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Alprazolam
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA207507
- Marketing category
- ANDA
- Marketing start
- 2018-07-09
- Marketing end
- 0000-00-00
- Substance
- ALPRAZOLAM
- Active strength
- 1 mg/1
- Pharmacologic classes
- Benzodiazepine [EPC],Benzodiazepines [CS]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5261 | ALPRAZOLAM TABLET [A-S MEDICATION SOLUTIONS] | 8 | Legacy NDC | 20230513_d2ff7095-ee9a-4034-854f-efcfec47b284.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5261-0 | 50090526100 | 30 TABLET in 1 BOTTLE (50090-5261-0) | 30 tablet | 2020-10-15 | 0000-00-00 | No | No | Current |
| 50090-5261-1 | 50090526101 | 20 TABLET in 1 BOTTLE (50090-5261-1) | 20 tablet | 2020-10-15 | 0000-00-00 | No | No | Current |
| 50090-5261-2 | 50090526102 | 60 TABLET in 1 BOTTLE (50090-5261-2) | 60 tablet | 2020-10-15 | 0000-00-00 | No | No | Current |
| 50090-5261-3 | 50090526103 | 90 TABLET in 1 BOTTLE (50090-5261-3) | 90 tablet | 2020-10-15 | 0000-00-00 | No | No | Current |